SE-ATLAS

Hereditary ataxia Friedreich ataxia Autosomal dominant cerebellar ataxia Rare ataxia Autosomal dominant cerebellar ataxia type I Lambert-Eaton myasthenic syndrome Autosomal dominant cerebellar ataxia type IV Autosomal dominant cerebellar ataxia type III Leukodystrophy Motor neuron disease ATTRV30M amyloidosis Wilson disease Hereditary spastic paraplegia Myasthenia gravis Congenital myasthenic syndrome Hereditary sodium channelopathy-related small fibers neuropathy Neuromuscular disease Acute pandysautonomia Muscular dystrophy Huntington disease Hereditary sensory and autonomic neuropathy Mutilating hereditary sensory neuropathy with spastic paraplegia Pure autonomic failure Dural sinus malformation Isolated dystonia Autosomal dominant cerebellar ataxia type II Rare disorder with dystonia and other neurologic or systemic manifestation Rare dystonia Amyotrophic lateral sclerosis Multifocal motor neuropathy Spinocerebellar ataxia type 29 Spinocerebellar ataxia type 38 Spinocerebellar ataxia type 34 Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy Spinocerebellar ataxia type 41 Spinocerebellar ataxia type 42 Spinocerebellar ataxia type 31 Spinocerebellar ataxia type 37 Spinocerebellar ataxia type 1 Spinocerebellar ataxia type 3 Spinocerebellar ataxia type 2 Spinocerebellar ataxia type 17 Spinocerebellar ataxia type 6 Spinocerebellar ataxia type 10 Spinocerebellar ataxia type 8 Spinocerebellar ataxia type 14 Spinocerebellar ataxia type 30 Spinocerebellar ataxia type 12 Spinocerebellar ataxia type 4 Spinocerebellar ataxia type 27 Spinocerebellar ataxia type 11 Spinocerebellar ataxia type 5 Spinocerebellar ataxia type 15/16 Spinocerebellar ataxia type 13 Spinocerebellar ataxia type 18 Spinocerebellar ataxia type 19/22 Spinocerebellar ataxia type 45 Familial dysautonomia Spinocerebellar ataxia type 40 Spinocerebellar ataxia type 28 Spinocerebellar ataxia type 23 Spinocerebellar ataxia type 25 Spinocerebellar ataxia type 26 Spinocerebellar ataxia type 32 Spinocerebellar ataxia type 21 Spinocerebellar ataxia type 46 Spinocerebellar ataxia type 36 Spinocerebellar ataxia type 43 Spinocerebellar ataxia type 35 Chronic inflammatory demyelinating polyneuropathy Spinocerebellar ataxia type 20 Proximal spinal muscular atrophy type 1 Skeletal muscle disease Genetic skeletal muscle disease Acquired skeletal muscle disease Neuromuscular junction disease Genetic neuromuscular junction disease Acquired neuromuscular junction disease Genetic peripheral neuropathy Rare peripheral neuropathy Acquired peripheral neuropathy Proximal spinal muscular atrophy Proximal spinal muscular atrophy type 3 Proximal spinal muscular atrophy type 2 Proximal spinal muscular atrophy type 4